Influence of the Composition of Temporary Restorative Material in Vital Teeth

F

Federal University of Uberlandia

Status

Unknown

Conditions

MTA
Dental Restoration, Temporary

Treatments

Procedure: Carie removal
Procedure: Finishing the temporary direct restoration
Procedure: Manipulation of the temporary material based on Mineral trioxide aggregate
Procedure: Material insertion on the cavity
Procedure: Manipulation of the temporary material based on Zinc Oxide and Eugenol
Procedure: Relative isolation

Study type

Interventional

Funder types

Other

Identifiers

NCT03437655
2.358.776

Details and patient eligibility

About

The aim of this study is through a randomized clinical trial, double blind, splithmouth, evaluate the success rate (retation rate and dental sensibility) of temporary direct restorations in vital teeth. The composition of the temporary direct restoration (based on Zinc-Oxide with Eugenol; and mineral trioxide aggregate). Data will be collected, tabulated and submitted to statistical analysis.

Full description

The confection of temporary direct restoration is still verry commom in dental clinic routine, either by the time required or by biological requirements.The temporary restorations must have sufficient retention and solubility between the consultation intervals to avoid displacement and infiltration; besides being biocompatible to avoid sensitivity. The aim of this study is through a randomized clinical trial, double blind, splithmouth, evaluate the success rate (retention rate and dental sensibility) of temporary direct restoration on vital teeth. The composition of the temporary material (based on Zinc-Oxide with Eugenol; and based on mineral trioxide aggregate) will be evaluated. Twenty-five participants with at least two vital teeth with the need to confection of direct restoration (each participant) will be selected. The teeth will be randomly divided into 2 different groups according to the temporary material composition (Based on Zinc-Oxide with Eugenol; and based on mineral trioxide aggregate). Data will be collected, tabulated and submitted to statistical analysis.

Enrollment

25 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Healthy volunteers; both genres; presence of at least two teeth with indication of direct restoration; good oral hygiene.

Exclusion criteria

Dentures or orthodontics; presence of periodontal disease and,or parafunctional habits; systemic disease and, or severe psychological; constant use of analgesic and, or anti-inflammatory or allergic response to dental products.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

25 participants in 2 patient groups

Zinc oxide and eugenol
Active Comparator group
Description:
Temporary direct restoration with zinc oxide and eugenol.
Treatment:
Procedure: Manipulation of the temporary material based on Zinc Oxide and Eugenol
Procedure: Relative isolation
Procedure: Material insertion on the cavity
Procedure: Finishing the temporary direct restoration
Procedure: Carie removal
Mineral trioxide aggregate
Active Comparator group
Description:
Temporary direct restoration with Mineral trioxide aggregate.
Treatment:
Procedure: Relative isolation
Procedure: Material insertion on the cavity
Procedure: Manipulation of the temporary material based on Mineral trioxide aggregate
Procedure: Finishing the temporary direct restoration
Procedure: Carie removal

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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